BEUDAMED
    5 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014

    X3 TRIATHLON CS INS SIZE 4 9MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·May 14, 2013

    COBE SPECTRA SEAL SAFE

    FDA Adverse Event
    Other ·CARIDIANBCT·Product code LKN·May 17, 2011

    INNOVA 2100

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS SCS·Product code MQB·August 13, 2008

    BD PYXIS¿ ANESTHESIA STATION ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·July 17, 2025